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Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A
Concanavalin A stimulation of T-cell cytotoxicity has been shown to be absolutely dependent on helper T-cell collaboration. Thymocytes stimulated with ConA do not differentiate to yield cytotoxic effector cells. However, thymocytes cocultured with irradiated spleen cells as helpers and ConA yield hi...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1977
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180654/ https://www.ncbi.nlm.nih.gov/pubmed/300781 |
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collection | PubMed |
description | Concanavalin A stimulation of T-cell cytotoxicity has been shown to be absolutely dependent on helper T-cell collaboration. Thymocytes stimulated with ConA do not differentiate to yield cytotoxic effector cells. However, thymocytes cocultured with irradiated spleen cells as helpers and ConA yield high levels of cytotoxicity. The helper cell bears theta antigens on its surface, is not an adherent cell, and does not require any adherent cell functions in our culture conditions. The ConA-dependent helper cells appear to be polyclonal in specificity. Thus, polyclonal stimulation of cytotoxicity by ConA requires T helper- T precursor collaboration in analogy to antigen-specific T helper-T precursor interactions. Unlike the antigen-specific interacitons, the ConA-driven cytotoxicity does not appear to require linked associative recognition for induction of cytotoxicity. |
format | Text |
id | pubmed-2180654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21806542008-04-17 Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A J Exp Med Articles Concanavalin A stimulation of T-cell cytotoxicity has been shown to be absolutely dependent on helper T-cell collaboration. Thymocytes stimulated with ConA do not differentiate to yield cytotoxic effector cells. However, thymocytes cocultured with irradiated spleen cells as helpers and ConA yield high levels of cytotoxicity. The helper cell bears theta antigens on its surface, is not an adherent cell, and does not require any adherent cell functions in our culture conditions. The ConA-dependent helper cells appear to be polyclonal in specificity. Thus, polyclonal stimulation of cytotoxicity by ConA requires T helper- T precursor collaboration in analogy to antigen-specific T helper-T precursor interactions. Unlike the antigen-specific interacitons, the ConA-driven cytotoxicity does not appear to require linked associative recognition for induction of cytotoxicity. The Rockefeller University Press 1977-05-01 /pmc/articles/PMC2180654/ /pubmed/300781 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A |
title | Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A |
title_full | Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A |
title_fullStr | Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A |
title_full_unstemmed | Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A |
title_short | Helper T cells are required for the polyclonal stimulation of cytotoxic T cells by concanavalin A |
title_sort | helper t cells are required for the polyclonal stimulation of cytotoxic t cells by concanavalin a |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180654/ https://www.ncbi.nlm.nih.gov/pubmed/300781 |